Hbs1ltm1c(KOMP)Wtsi
Targeted Allele Detail
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Symbol: |
Hbs1ltm1c(KOMP)Wtsi |
Name: |
Hbs1-like (S. cerevisiae); targeted mutation 1c, Wellcome Trust Sanger Institute |
MGI ID: |
MGI:6718578 |
Synonyms: |
Hbs1lfl |
Gene: |
Hbs1l Location: Chr10:21171876-21244788 bp, + strand Genetic Position: Chr10, 9.75 cM
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Alliance: |
Hbs1ltm1c(KOMP)Wtsi page
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IMPC: |
Hbs1l gene page |
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Mutant Cell Line: |
EPD0693_2_A02 |
Germline Transmission: |
Earliest citation of germline transmission:
J:306384
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Parent Cell Line: |
JM8A3.N1 (ES Cell)
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Strain of Origin: |
C57BL/6N-Atm1Brd
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Project Collection: |
KOMP-CSD
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Allele Type: |
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Targeted (Conditional ready, No functional change) |
Mutation: |
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Insertion
Vector: L1L2_Bact_P
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Mutation details: The L1L2_Bact_P cassette was inserted at position 21212311 of Chromosome 10 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of the targeted exon(s) at position 21213197. The critical exon(s) is/are thus flanked by loxP sites. A "conditional ready" (floxed) allele can be created by flp recombinase expression in mice carrying this allele. Subsequent cre expression results in a knockout mouse. If cre expression occurs without flp expression, a reporter knockout mouse will be created. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml
(J:306384)
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View phenotypes and curated references for all genotypes (concatenated display).
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Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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Carrying any Hbs1l Mutation: |
51 strains or lines available
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Original: |
J:306384 Terrey M, et al., Defects in translation-dependent quality control pathways lead to convergent molecular and neurodevelopmental pathology. Elife. 2021 Apr 26;10:e66904 |
All: |
1 reference(s) |
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